NCT07137143 The Effect of Heating the Intensive Care Room in the Early Postoperative Period on Patient Outcomes
| NCT ID | NCT07137143 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Cukurova University |
| Condition | Abdominal Surgery Complications |
| Study Type | INTERVENTIONAL |
| Enrollment | 70 participants |
| Start Date | 2025-04-20 |
| Primary Completion | 2025-10-30 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 70 participants in total. It began in 2025-04-20 with a primary completion date of 2025-10-30.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The aim of this study was to evaluate the effect of heating the intensive care room in the early postoperative period on patient outcomes.
Eligibility Criteria
Inclusion Criteria: * The following criteria will be included in the sample: * Patients who underwent elective abdominal surgery and were admitted to intensive care after surgery. * Patients aged 18 and over. * Patients whose body temperature on the morning of surgery was neither below 36°C nor above 37.5°C. * Patients who did not have a pacemaker, dementia, advanced spasticity, muscle atrophy, peripheral lesions, osteoporosis, skin irritation, diabetes, hypertension, or obesity. * Patients who did not require mechanical ventilation. * Patients who did not have any illness that would impair thermoregulation (such as head trauma or hypothalamic damage). • Patients who were not taking medications that would affect thermoregulation, such as vasodilators. * Patients who did not have peripheral circulation problems. * Patients who were not alcohol or substance abusers. * Patients who did not have mental retardation. * Patients who were conscious and oriented to person, time, and place. * Patients who could speak Turkish. * Patients who did not have any auditory or visual impairments. * Patients who volunteered for the study. Exclusion Criteria: * Patients who do not meet the sampling criteria, who develop postoperative complications (bleeding, intubation, stenosis, necrosis, ileus, dermatitis, parastomal herniation, etc.), and whose relatives do not consent to the study will not be included in the study.
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07137143 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Abdominal Surgery Complications. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07137143 currently recruiting?
Yes, NCT07137143 is actively recruiting participants. Contact the research team at cansel9815@gmail.com for enrollment information.
Where is the NCT07137143 trial being conducted?
This trial is being conducted at Adana, Turkey (Türkiye).
Who is sponsoring the NCT07137143 clinical trial?
NCT07137143 is sponsored by Cukurova University. The trial plans to enroll 70 participants.